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Clinical Trial Summary

This non-randomised, prospective trial will examine the feasibility and efficacy of VT ablation guided by activation mapping using the Octaray and Optrell catheters. Annotation algorithms within the CARTO3 electro-anatomical mapping system will be integrated with 3D scar segmentation data from cardiac MRI (ADAS-VT), and extrastimulus voltage mapping will identify sites of interest for focussed activation mapping. The investigators hypothesise that the examination of these data will identify critical target sites for ablation. Intra-procedural diagnostic performance of the Octaray and Optrell catheters will be assessed as the primary outcome, and will be compared with the standard of care. Secondary, clinical outcomes - primarily the need for ICD therapies at 12 months post ablation - will be compared with propensity-matched controls undergoing substrate-based ablation alone. Follow-up MRI scans will review the impact of ablation on the elimination of conduction channels.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05152784
Study type Interventional
Source Barts & The London NHS Trust
Contact Pier D Lambiase, MBBS
Phone 02073 777000
Email p.lambiase@ucl.ac.uk
Status Recruiting
Phase N/A
Start date November 21, 2022
Completion date October 3, 2025

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